Second-line treatment of non-small cell lung cancer by biweekly gemcitabine and docetaxel plus /- granulocyte-macrophage colony stimulating factor and low dose aldesleukine

被引:19
作者
Correale, Pierpaolo [2 ]
Miano, Salvatora Tindara [2 ]
Remondo, Cinzia [2 ]
Migali, Cristina [2 ]
Rotundo, Maria Saveria [1 ,3 ]
Macri, Paolo [4 ,5 ]
Tagliaferri, Pierosandro [1 ,3 ]
Tassone, Pierfrancesco [1 ,3 ]
Caraglia, Michele [6 ]
Gotti, Giuseppe [7 ]
Francini, Guido [2 ]
机构
[1] Magna Graecia Univ Catanzaro, Med Oncol Unit, Catanzaro, Italy
[2] Univ Siena, Sch Med, Sect Med Oncol, Dept Giorgio Segre Pharmacol, I-53100 Siena, Italy
[3] Magna Graecia Univ Catanzaro, Reg Ctr Genet Counselling & Innovat Therapies Med, Catanzaro, Italy
[4] Magna Graecia Univ Catanzaro, Thorac Surg Oncol Unit, Catanzaro, Italy
[5] Canc Ctr Tommaso Campanella, Catanzaro, Italy
[6] Univ Naples 2, Dept Biochem & Biophys F Cedrangolo, Naples, Italy
[7] Univ Siena, Sch Med, Thorac Surg Unit, I-53100 Siena, Italy
关键词
non-small cell lung cancer; gemcitabine; docetaxel; granulocyte-macrophage colony stimulating factor; aldesleukine; Phase II; second-line chemoimmunotherapy; ANTITUMOR-ACTIVITY; PACLITAXEL; CARCINOMA; TRIAL; CHEMOIMMUNOTHERAPY; TAXOL;
D O I
10.4161/cbt.8.6.7593
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The antitumor activity of a novel biweekly gemcitabine (G) + docetaxel (D) regimen +/- granulocyte-macrophage colony stimulating factor (GM-CSF) and aldesleukine (IL-2) has been evaluated in a phase II trial in advanced pretreated non-small cell lung cancer (NSCLC). Results: The treatment was well tolerated. The 42.3% response rate exceeded the predefined target activity, while time to progression (TTP) and overall survival (OS) were 7 and 11.2 months, respectively. A greater objective response rate (58.3% vs. 28.6%) and an increased number of eosinophils, basophils and activated mononuclear blood cells were observed in those patients who also received cytokine administration. Methods: Twenty-six NSCLC patients received second line G (1,000 mg/m(2)) and D (75 mg/m(2)) every 15 days. 12/26 patients also received s.c. GM-CSF (100 mu g, days 2-6) and s.c. IL-2 (0.5 MIU/twice daily, days 7-14 and 16-29) by random selection. Conclusion: The biweekly GD regimen is a safe and active second-line treatment in NSCLC. Addition of immune-adjuvant cytokines' may enhance the activity of this therapeutic combination.
引用
收藏
页码:497 / 502
页数:6
相关论文
共 31 条
[1]   Treatment of human colon carcinoma cell lines with anti-neoplastic agents enhances their lytic sensitivity to antigen-specific CD8+ cytotoxic T lymphocytes [J].
Bergmann-Leitner, ES ;
Abrams, SI .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2001, 50 (09) :445-455
[2]   The immunological effects of taxanes [J].
Chan, OTM ;
Yang, LX .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2000, 49 (4-5) :181-185
[3]   Dendritic cell-mediated cross-presentation of antigens derived from colon carcinoma cells exposed to a highly cytotoxic multidrug regimen with gemcitabine, oxaliplatin, 5-fluorouracil, and leucovorin, elicits a powerful human antigen-specific CTL response with antitumor activity in vitro [J].
Correale, P ;
Cusi, MG ;
Del Vecchio, MT ;
Aquino, A ;
Prete, S ;
Tsang, KY ;
Micheli, L ;
Nencini, C ;
La Placa, M ;
Montagnani, F ;
Terrosi, C ;
Caraglia, M ;
Formica, V ;
Giorgi, G ;
Bonmassar, E ;
Francini, G .
JOURNAL OF IMMUNOLOGY, 2005, 175 (02) :820-828
[4]   Chemo-immunotherapy of metastatic colorectal carcinoma with gemcitabine plus FOLFOX 4 followed by subcutaneous granulocyte macrophage colony-stimulating factor and interleukin-2 induces strong immunologic and antitumor activity in metastatic colon cancer patients [J].
Correale, P ;
Cusi, MG ;
Tsang, KY ;
Del Vecchio, MT ;
Marsili, S ;
La Placa, M ;
Intrivici, C ;
Aquino, A ;
Micheli, L ;
Nencini, C ;
Ferrari, F ;
Giorgi, G ;
Bonmassar, E ;
Francini, G .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (35) :8950-8958
[5]   Recruitment of dendritic cells and enhanced antigen-specific immune reactivity in cancer patients treated with hr-GM-CSF (Molgramostim) and hr-IL-2: results from a phase Ib clinical trial [J].
Correale, P ;
Campoccia, G ;
Tsang, KY ;
Micheli, L ;
Cusi, MG ;
Sabatino, M ;
Bruni, G ;
Sestini, S ;
Petrioli, R ;
Pozzessere, D ;
Marsili, S ;
Fanetti, G ;
Giorgi, G ;
Francini, G .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (07) :892-902
[6]   Chemotherapeutic drugs may be used to enhance the killing efficacy of human tumor antigen peptide-specific CTLs [J].
Correale, Pierpaolo ;
Del Vecchio, Maria Teresa ;
La Placa, Marco ;
Montagnani, Francesco ;
Di Genova, Giuseppa ;
Savellini, Gianni Gori ;
Terrosi, Chiara ;
Mannucci, Susanna ;
Giorgi, Giorgio ;
Francini, Guido ;
Cusi, Maria Grazia .
JOURNAL OF IMMUNOTHERAPY, 2008, 31 (02) :132-147
[7]  
ERLICHMAN C, 1991, Current Opinion in Oncology, V3, P1037, DOI 10.1097/00001622-199112000-00011
[8]  
Ferlay J., 2001, CANC INCIDENCE MORTA
[9]  
GAO G, 2007, LUNG CANCER, V57, P348
[10]   THE TAXOIDS - PACLITAXEL AND DOCETAXEL [J].
GELMON, K .
LANCET, 1994, 344 (8932) :1267-1272